Disease: Myocardial Infarction ×
Source: BEFREE ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3846662
rs3846662
Entrez Id: 3156
Gene Symbol: HMGCR
HMGCR
CUI: C0027051
Disease:
Myocardial Infarction 		0.010 GeneticVariation BEFREE The LDL-associated SNP, rs3846662, appears to confer susceptibility to MI in Japanese. 20145341 2010